5934-57-6 Usage
Chemical structure
A complex chemical compound with several functional groups, including a phenyl ring, a morpholine group, a thiomorpholine group, and a pyrrolidine-2,5-dione ring.
Substitution pattern
The phenyl ring is substituted with a morpholine group and a thiomorpholine group.
Linkage
The morpholine group is attached to the phenyl ring via a sulfonyl linkage, and the thiomorpholine group is attached to the pyrrolidine-2,5-dione ring.
Potential applications
Organic synthesis and drug development due to its unique and diverse chemical structure.
Further research
Additional research and analysis are required to fully understand the properties and potential uses of this compound.
Functional groups
Contains a sulfonyl group, which is a sulfur-oxygen linkage, and two heterocyclic amine groups (morpholine and thiomorpholine).
Molecular weight
Approximately 430.56 g/mol (calculated from the molecular formula)
Stability
The stability of the compound is not explicitly mentioned, but the presence of multiple heteroatoms and a complex structure may suggest that it could be sensitive to certain reaction conditions or degradation pathways.
Reactivity
The compound's reactivity profile is not provided, but the presence of various functional groups may indicate potential reactivity with certain reagents or under specific conditions.
Structural complexity
The compound has a relatively high degree of structural complexity due to the presence of multiple heteroatoms, a phenyl ring, and two heterocyclic amine groups.
Synthesis
The synthesis of this compound likely involves multiple steps, including the formation of the sulfonyl linkage and the attachment of the morpholine and thiomorpholine groups to the phenyl and pyrrolidine-2,5-dione rings, respectively.
Analytical techniques
Techniques such as NMR, mass spectrometry, and elemental analysis would be useful for characterizing and confirming the structure of this compound.
Safety considerations
As with any new chemical compound, safety precautions should be taken when handling and studying 1-[4-(morpholin-4-ylsulfonyl)phenyl]-3-thiomorpholin-4-ylpyrrolidine-2,5-dione, including proper storage, handling, and disposal procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 5934-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5934-57:
(6*5)+(5*9)+(4*3)+(3*4)+(2*5)+(1*7)=116
116 % 10 = 6
So 5934-57-6 is a valid CAS Registry Number.
5934-57-6Relevant articles and documents
Synthesis and structural studies of 1-amino-1-deoxy-α-L-xylo-hexulopyranose: L-Sorbosamine
Mossine, Valeri V.,Byrne, Todd S.,Barnes, Charles L.,Mawhinney, Thomas P.
, p. 153 - 162 (2018)
Ketosamines are an important class of glycoconjugates widely employed in clinical diagnostics and implicated in development of diabetic complications, intestinal infections, or advanced cancer, as well as in food organoleptic and nutritional value. We report on the first preparation and structural characterization of 1-amino-1-deoxy-L-sorbose (L-sorbosamine, L-SorNH2). The monosaccharide was synthesized from L-sorbose following a classic phenylosazone protocol. In aqueous solution, L-SorNH2 assumes an anomeric equilibrium consisting of 89.3% α-pyranose, 3.7% β-pyranose, 3.8% α-furanose, 2.4% β-furanose, and 0.9% acyclic keto tautomer. The α-pyranose anomer in crystalline L-SorNH2 × HCl adopts the 2C5 chair conformation, with bond lengths and valence angles comparing well with related sorbopyranose structures. All hydroxyl oxygen atoms, the ammonium group and chloride ion are involved in an extensive hydrogen bonding network which is formed by infinite chains with fused antidromic R7 6(14), R5 4(10), and R4 3(8) cycles. The Hirshfeld surface analysis suggests a significant contribution of the non-polar intermolecular contacts to the crystal structure, as well.
